A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019259



Internal ID19108477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116260580..116289548hg38UCSC Ensembl
Innerchr5:115596277..115625245hg19UCSC Ensembl
Innerchr5:115624176..115653144hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3828969
hg1928969
hg1828969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5792n100
Supporting Variantsnssv3647149, nssv3647157, nssv3647158, nssv3647164, nssv3647151, nssv3647144, nssv3647152, nssv3647141, nssv3647132, nssv3647171, nssv3647176, nssv3647142, nssv3647153, nssv3647178, nssv3647146, nssv3647168, nssv3647180, nssv3647155, nssv3647136, nssv3647138, nssv3647150, nssv3647181, nssv3647154, nssv3647137, nssv3647163, nssv3647161, nssv3647167, nssv3647174, nssv3647139, nssv3647172, nssv3647145, nssv3647143, nssv3647173, nssv3647179, nssv3647175, nssv3647169, nssv3647148, nssv3647160, nssv3647162, nssv3647159, nssv3647133, nssv3647166, nssv3647156, nssv3647134, nssv3647147, nssv3647170, nssv3647140, nssv3647177, nssv3647135, nssv3647165
Samples
Known GenesCOMMD10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019259
Frequency
Sample Size11257
Observed Gain0
Observed Loss50
Observed Complex0
Frequencyn/a


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